NDC 63629-9474 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63629-9474

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076433
Marketed since
June 1, 2017
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (1)

Package NDCDescriptionSince
63629-9474-190 TABLET, FILM COATED in 1 BOTTLE (63629-9474-1)Nov 28, 2022

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